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催化学报  2013 

离子液体催化吲哚羟烷基化反应

DOI: 10.1016/S1872-2067(12)60571-3, PP. 1187-1191

Keywords: 离子液体,吲哚,环状碳酸酯,羟烷基化

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Abstract:

?报道了咪唑类离子液体催化吲哚和环状碳酸酯反应合成羟烷基吲哚,系统考察了反应时间、催化剂用量、反应温度和反应物比例对离子液体催化反应性能的影响.在优化的反应条件下,吲哚与碳酸乙烯酯或碳酸丙烯酯反应可高效地生成1-(2-羟乙基)吲哚、1-(2-羟丙基)吲哚及其相应的衍生物.离子液体的催化活性与离子液体中的阴离子有关,其催化活性顺序为BF4-﹤Br-﹤Cl-﹤OAc-,与阴离子的碱度顺序一致.

References

[1]  Palgunadi J, Hong S Y, Lee J K, Lee H D, Lee S, Cheong M, Kim H S. J Phys Chem B, 2011, 115: 1067
[2]  Kinage A K, Gupte S P, Chaturvedi R K, Chaudhari R V. Catal Commun, 2008, 9: 1649
[3]  Tang L, Yu J H, Wu H S, Fan H X, Yang Y S, Ji R Y. Eur J Med Chem, 2008, 43: 1997
[4]  Lohray B B, Bhushan V, Rao B P, Madhavan G R, Murali N, Rao K N, Reddy A K, Rajesh B M, Reddy P G, Chakrabarti R, Vikramadithyan R K, Rajagopalan R, Mamidi R N V S, Jajoo H K, Subramaniam S. J Med Chem, 1998, 41: 1619
[5]  Schiffner J A, W?ste T H, Oestreich M. Eur J Org Chem, 2010, 2010: 174
[6]  Padwa A, Hertzog D L, Nadler W R. J Org Chem, 1994, 59: 7072
[7]  Gu Y, Ogawa C, Kobayashi S. Org Lett, 2007, 9: 175
[8]  Li Z, Qin J G, Li S J, Ye C, Luo J, Cao Y. Macromolecules, 2002, 35: 9232
[9]  Li Z, Gong W, Qin J G, Yang Z, Ye C. Polymer, 2005, 46: 4971
[10]  Li Q Q, Li Z, Zeng F X, Gong W, Li Z A, Zhu Z C, Zeng Q, Yu S S, Ye C, Qin J G. J Phys Chem B, 2007, 111: 508
[11]  Bloxham J, Moody C J, Slawin A M Z. Tetrahedron, 2002, 58: 3709
[12]  Giannessi F, Dell’uomo N, Tassoni E, Tinti M O, Sciarroni A F, Bandera M, Pessotto P, Arduini A. US Patent 0 027 098. 2008
[13]  Moon H, Hwang J, Kim N, Park S Y. Macromolecules, 2000, 33: 5116
[14]  Parrish J P, Salvatore R N, Jung K W. Tetrahedron, 2000, 56: 8207
[15]  Bai D S, Wang Q, Song Y Y, Li B, Jing H W. Catal Commun, 2011, 12: 684
[16]  Gao Z W, Xiao L F, Chen J, Xia C G. Chin J Catal (高志文, 肖林飞, 陈静, 夏春谷. 催化学报), 2008, 29: 831
[17]  Shivarkar A B, Gupte S P, Chaudhari R V. Synlett, 2006: 1374
[18]  Selva M, Perosa A, Fabris M. Green Chem, 2008, 10: 1068
[19]  Selva M, Fabris M, Lucchini V, Perosa A, Noe M. Org Biomol Chem, 2010, 8: 5187
[20]  Olivier-Bourbigou H, Magna L, Morvan D. Appl Catal A, 2010, 373: 1
[21]  Li J, Wang L Q, Shi F, Liu S M, He Y D, Lu L J, Ma X Y, Deng Y Q. Catal Lett, 2011, 141: 339
[22]  Cai Y Q, Lu Y, Liu Y, Gao G H. Catal Lett, 2007, 119: 154
[23]  Gu Y L, Li G X. Adv Synth Catal, 2009, 351: 817
[24]  Mo J, Xiao J L. Angew Chem Int Ed, 2006, 45: 4152
[25]  Mo J, Xu L J, Ruan J W, Liu S F, Xiao J L. Chem Commun, 2006: 3591
[26]  Leng Y, Zhao P P, Zhang M J, Chen G J, Wang J. Sci China Chem, 2012, 55: 1796
[27]  Cho H J, Kwon H M, Tharun J, Park D W. J Ind Eng Chem, 2010, 16: 679
[28]  Fu X L, Zhang Z, Li C M, Wang L B, Ji H Y, Yang Y, Zou T, Gao G H. Catal Commun, 2009, 10: 665
[29]  Zhang L F, Fu X L, Gao G H. ChemCatChem, 2011, 3: 1359
[30]  Zhang L F, Yang S J, Gao G H. Chin J Catal (张利锋, 杨四娟, 高国华. 催化学报), 2011, 32: 1875
[31]  Zhang L F, Yang Y, Xue Y R, Fu X L, An Y, Gao G H. Catal Today, 2010, 158: 279
[32]  Chu Y, Deng H, Cheng J P. J Org Chem, 2007, 72: 7790
[33]  Zhao H, Baker G A, Song Z Y, Olubajo O, Zanders L, Campbell S M. J Mol Catal B, 2009, 57: 149

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